GlyCosmos Portal

Source	Last Updated
GlyConnect	April 19, 2023
GlycoProtDB	October 1, 2021
GlyGen	June 4, 2024
The O-GlcNAc Database	June 3, 2024
UniProt	June 4, 2024

Displaying entries **276 - 300** of **18496** in total

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UniProt ID	Protein Name	Gene Symbol	Organism	No. of Glycosylation Sites ▼	No. of GlyTouCan IDs	Disease Ontology
O95817	BAG family molecular chaperone regulator 3	BAG3 BIS	Homo sapiens (human)	21	2
Q02505	Mucin-3A	MUC3A MUC3	Homo sapiens (human)	21	1
Q9UHD9	Ubiquilin-2	UBQLN2 N4BP4 PLIC2	Homo sapiens (human)	21	3
O94907	Dickkopf-related protein 1	DKK1	Homo sapiens (human)	21	1
Q76M96	Coiled-coil domain-containing protein 80	CCDC80 DRO1 URB	Homo sapiens (human)	21	7
Q14515	SPARC-like protein 1	SPARCL1	Homo sapiens (human)	20	19
Q96RV3	Pecanex-like protein 1	PCNX1 KIAA0805 KIAA0995 PCNX PCNXL1	Homo sapiens (human)	20	3
Q92854	Semaphorin-4D	SEMA4D C9orf164 CD100 SEMAJ	Homo sapiens (human)	20	41
P10253	Lysosomal alpha-glucosidase	GAA	Homo sapiens (human)	20	85	Becker muscular dystrophy Clouston syndrome Duchenne muscular dystrophy Fabry disease Friedreich ataxia 1 Friedreich ataxia aortic aneurysm ataxia telangiectasia atrial heart septal defect 1 atrial heart septal defect 2 atrial heart septal defect 3 atrial heart septal defect 4 atrial heart septal defect 5 atrial heart septal defect 6 atrial heart septal defect 7 atrial heart septal defect 8 atrial heart septal defect 9 atrial heart septal defect autosomal dominant limb-girdle muscular dystrophy type 1 autosomal dominant limb-girdle muscular dystrophy type 1H autosomal dominant limb-girdle muscular dystrophy type 2 autosomal dominant limb-girdle muscular dystrophy type 3 autosomal dominant limb-girdle muscular dystrophy autosomal recessive limb-girdle muscular dystrophy type 2A autosomal recessive limb-girdle muscular dystrophy type 2B autosomal recessive limb-girdle muscular dystrophy type 2C autosomal recessive limb-girdle muscular dystrophy type 2D autosomal recessive limb-girdle muscular dystrophy type 2E autosomal recessive limb-girdle muscular dystrophy type 2F autosomal recessive limb-girdle muscular dystrophy type 2G autosomal recessive limb-girdle muscular dystrophy type 2H autosomal recessive limb-girdle muscular dystrophy type 2I autosomal recessive limb-girdle muscular dystrophy type 2J autosomal recessive limb-girdle muscular dystrophy type 2K autosomal recessive limb-girdle muscular dystrophy type 2L autosomal recessive limb-girdle muscular dystrophy type 2M autosomal recessive limb-girdle muscular dystrophy type 2N autosomal recessive limb-girdle muscular dystrophy type 2O autosomal recessive limb-girdle muscular dystrophy type 2P autosomal recessive limb-girdle muscular dystrophy type 2Q autosomal recessive limb-girdle muscular dystrophy type 2S autosomal recessive limb-girdle muscular dystrophy type 2T autosomal recessive limb-girdle muscular dystrophy type 2U autosomal recessive limb-girdle muscular dystrophy type 2Y autosomal recessive limb-girdle muscular dystrophy cancer cardiomyopathy cerebellar ataxia cerebellar disease chylomicron retention disease cystinuria cytochrome-c oxidase deficiency disease diaphragm disease disease of metabolism distal myopathy endomyocardial fibrosis facioscapulohumeral muscular dystrophy familial hypertrophic cardiomyopathy familial periodic paralysis galactosemia glucosephosphate dehydrogenase deficiency glycogen storage disease II glycogen storage disease III glycogen storage disease IV glycogen storage disease IXa glycogen storage disease IXb glycogen storage disease IXc glycogen storage disease IXd glycogen storage disease Ia glycogen storage disease VI glycogen storage disease VII glycogen storage disease hypertrophic cardiomyopathy isolated elevated serum creatine phosphokinase levels limb-girdle muscular dystrophy lipid storage disease lysosomal storage disease membranous glomerulonephritis mitochondrial metabolism disease mitochondrial myopathy muscular dystrophy myopathy neurodegenerative disease neuromuscular disease obsolete autosomal dominant limb-girdle muscular dystrophy type 1A obsolete autosomal dominant limb-girdle muscular dystrophy type 1B obsolete autosomal dominant limb-girdle muscular dystrophy type 1C obsolete autosomal recessive limb-girdle muscular dystrophy type 2R oculopharyngeal muscular dystrophy patent foramen ovale peroxisome biogenesis disorder 7A primary immunodeficiency disease sensorineural hearing loss thyroid gland anaplastic carcinoma
Q6UN15	Pre-mRNA 3'-end-processing factor FIP1	FIP1L1 FIP1 RHE	Homo sapiens (human)	20	4
Q8WYP5	Protein ELYS	AHCTF1 ELYS TMBS62	Homo sapiens (human)	20	2
Q8TER0	Sushi, nidogen and EGF-like domain-containing protein 1	SNED1	Homo sapiens (human)	20	5
Q96PV0	Ras/Rap GTPase-activating protein SynGAP	SYNGAP1 KIAA1938	Homo sapiens (human)	20	1
Q6ZRP7	Sulfhydryl oxidase 2	QSOX2 QSCN6L1 SOXN	Homo sapiens (human)	20	7
P53708	Integrin alpha-8	ITGA8	Homo sapiens (human)	20	11
P26006	Integrin alpha-3	ITGA3 MSK18	Homo sapiens (human)	20	95
Q9Y6R7	IgGFc-binding protein	FCGBP	Homo sapiens (human)	20	47
Q9Y4D7	Plexin-D1	PLXND1 KIAA0620	Homo sapiens (human)	20	24
P05783	Keratin, type I cytoskeletal 18	KRT18 CYK18	Homo sapiens (human)	20	6
Q9NYQ7	Cadherin EGF LAG seven-pass G-type receptor 3	CELSR3 CDHF11 EGFL1 FMI1 KIAA0812 MEGF2	Homo sapiens (human)	20	4
O15031	Plexin-B2	PLXNB2 KIAA0315	Homo sapiens (human)	20	160
P27918	Properdin	CFP PFC	Homo sapiens (human)	20	1
Q6ZRS2	Helicase SRCAP	SRCAP KIAA0309	Homo sapiens (human)	20	5
Q9UIQ6	Leucyl-cystinyl aminopeptidase	LNPEP OTASE	Homo sapiens (human)	20	58
O15027	Protein transport protein Sec16A	SEC16A KIAA0310 SEC16 SEC16L	Homo sapiens (human)	20	1

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